Repetitive transcranial magnetic stimulation inhibits Sirt1/MAO-A signaling in the prefrontal cortex in a rat model of depression and cortex-derived astrocytes

Mol Cell Biochem. 2018 May;442(1-2):59-72. doi: 10.1007/s11010-017-3193-8. Epub 2017 Sep 25.

Abstract

Repetitive transcranial magnetic stimulation (rTMS) is a useful monotherapy for depression or adjunctive therapy for resistant depression. However, the anti-depressive effects of different parameters and the underlying mechanisms remain unclear. Here, we aimed to assess the effect of rTMS with different parameters (1/5/10 Hz, 0.84/1.26 T) on the depressive-like behaviors, 5-hydroxytryptamine (5-HT), 5-HIAA (5-hydroxyindoleacetic acid) and DA and NE levels, and monoamine oxidase A (MAO-A) activity in chronic unpredictable stress-treated rats, along with the expression of sirtuin 1 (Sirt1) and MAO-A in the prefrontal cortex (PFC) and cortex-derived astrocytes from new-born rats. Moreover, the depressive-like behaviors were monitored following the transcranial injection of the Sirt1 inhibitor EX527 (1 mM) daily for 1 week. We found that rTMS treatment (5/10 Hz, 0.84/1.26 T) ameliorated depressive-like behaviors, increased 5-HT, DA and NE levels, decreased the 5-HIAA level and Sirt1 and MAO-A expression, and reduced MAO-A activity in the PFC. The depressive-like behaviors were also ameliorated after the transcranial injection of EX527. Importantly, rTMS (5/10 Hz, 0.84/1.26 T) inhibited Sirt1 and MAO-A expressions in astrocytes and Sirt1 knockdown with short hairpin RNA decreased MAO-A expression in astrocytes. These results suggest that the inhibition of Sirt1/MAO-A expression in astrocytes in the PFC may contribute to the different anti-depressive effects of rTMS with different parameters, and may also provide a novel insight into the mechanisms underlying major depressive disorder.

Keywords: Astrocytes; CUS; Sirt1/MAO-A; rTMS.

MeSH terms

  • Animals
  • Astrocytes / enzymology*
  • Astrocytes / pathology
  • Behavior, Animal
  • Depression / enzymology*
  • Depression / pathology
  • Disease Models, Animal
  • Monoamine Oxidase / metabolism*
  • Prefrontal Cortex / enzymology*
  • Prefrontal Cortex / pathology
  • Rats
  • Signal Transduction*
  • Sirtuin 1 / metabolism*
  • Transcranial Magnetic Stimulation*

Substances

  • Monoamine Oxidase
  • Sirt1 protein, rat
  • Sirtuin 1